Pfizer Scientist, QC in St Louis, Missouri
The qualified candidate will join the Analytical R&D organization to enable development of biological therapeutics in Chesterfield, MO. The qualified candidate will be responsible for applying analytical methods in the assessment of product quality, biological activity, detection of impurities and characterization. This group performs testing in the R&D and/or regulated settings in support of clinical drug candidates. The group also supports method development, transfer, verification, qualification and validation as well as troubleshooting.
The qualified colleague is responsible for developing, troubleshooting and utilizing analytical methodologies to support GMP release and stability testing of clinical supplies.
The individual is responsible for becoming proficient in a breadth of analytical methodologies including Compendial test methods, HPLC, electrophoresis, residual DNA using qPCR, and ELISA.
The colleague must work within corporate guidelines and must appropriately record, archive and report all data.
The colleague must be able to interact effectively with peers and leaders as part of a multi-disciplinary team across multiple geographies.
The candidate must thrive in a fast-paced environment. Attention to detail, strong organizational skills, the ability to multitask and effective interpersonal, influencing skills and communication skills are required.
Experience with qPCR analysis and analytical testing of gene therapy therapeutics would be an advantage.
Education & Experience
MINIMUM: BS in chemistry, analytical chemistry, biochemistry, biology or related field
Minimum of three years of laboratory experience in a variety of large molecule and vaccine analytical techniques including experience with qPCR analysis. Ability to follow established procedures under minimal supervision.
DESIRABLE: Experience with Quality Systems in a GMP environment. Experience with method development over a wide variety of large molecule technologies including residual DNA using qPCR. Some knowledge of drug development process for progression of biological candidates.
OTHER ATTRIBUTES DESIRABLE:
•Excellent documentation skills
•Self-motivated and highly effective in a team-based environment
•Effective oral and written communication skills
•Experience in analysis of large molecules
•Experience with laboratory data systems such as Empower, and Laboratory Information Management Systems
There is no relocation available for this position.
Position requires occasional light lifting and periods of standing, sitting or walking.
Eligible for employee referral.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.
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Additional Offer Details:
Additional Location Information : St. Louis, MO Chesterfield
Eligible for Employee Referral Bonus
A career at Pfizer offers opportunity, ownership and impact.
All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the bio-pharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.